Triple

T22821290
Position Surface form Disambiguated ID Type / Status
Subject TRUPACT-II shipping casks E565234 entity
Predicate documentation P4310 FINISHED
Object Safety Analysis Report for Packaging (SARP) NE NERFINISHED

How this triple was built (3 steps)

Every LLM step that produced this triple, in pipeline order — named-entity classification, the disambiguation choices (the exact options shown, with the pick highlighted), and the generated description. The batch + timestamp of each is in the Provenance table below.

NER Named-entity recognition gpt-5-mini
Instruction
Given a phrase, classify it is english named entity (e.g., persons, organizations, works of art) in Latin script, or not (e.g., literals, dates, URLs, verbose phrases). For disambiguation, the statement where the phrase occurs as object is also given. Please return a JSON object with `phrase` (string, the phrase being analyzed) and `is_ne` (boolean, indicating whether the phrase is a Named Entity).
Input
Phrase: Safety Analysis Report for Packaging (SARP) | Statement: [TRUPACT-II shipping casks, documentation, Safety Analysis Report for Packaging (SARP)]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Safety Analysis Report for Packaging (SARP)
Context triple: [TRUPACT-II shipping casks, documentation, Safety Analysis Report for Packaging (SARP)]
  • A. Office of Safety Data and Analysis
    The Office of Safety Data and Analysis is a division within the U.S. Bureau of Transportation Statistics that specializes in collecting, analyzing, and disseminating data related to transportation safety.
  • B. Hazard Ranking System
    The Hazard Ranking System is a scoring tool used by the U.S. Environmental Protection Agency to assess the relative risk of contaminated sites and determine which ones qualify for inclusion on the Superfund National Priorities List.
  • C. ICH Harmonised Tripartite Guideline E2D Post-Approval Safety Data Management: Definitions and Standards for Expedited Reporting
    ICH E2D is an international regulatory guideline that standardizes how post-approval drug safety data are defined, managed, and rapidly reported to health authorities to ensure ongoing monitoring of medicinal product safety.
  • D. ICH S7A Safety Pharmacology Studies for Human Pharmaceuticals
    ICH S7A Safety Pharmacology Studies for Human Pharmaceuticals is an international guideline that outlines the core nonclinical safety pharmacology studies needed to evaluate the potential undesirable effects of new drugs on vital physiological functions before human use.
  • E. Safeguards Analytical Laboratory
    The Safeguards Analytical Laboratory is an International Atomic Energy Agency (IAEA) facility that performs nuclear material and environmental sample analysis to support global nuclear safeguards and non-proliferation verification.
  • F. None of above. chosen
  • G. Unsure - the case is ambiguous/there is not enough information to decide.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: Safety Analysis Report for Packaging (SARP)
Target entity description: The Safety Analysis Report for Packaging (SARP) is a comprehensive technical document that evaluates and demonstrates the safety and regulatory compliance of a specific packaging system used to transport radioactive or hazardous materials.
  • A. Office of Safety Data and Analysis
    The Office of Safety Data and Analysis is a division within the U.S. Bureau of Transportation Statistics that specializes in collecting, analyzing, and disseminating data related to transportation safety.
  • B. Hazard Ranking System
    The Hazard Ranking System is a scoring tool used by the U.S. Environmental Protection Agency to assess the relative risk of contaminated sites and determine which ones qualify for inclusion on the Superfund National Priorities List.
  • C. ICH Harmonised Tripartite Guideline E2D Post-Approval Safety Data Management: Definitions and Standards for Expedited Reporting
    ICH E2D is an international regulatory guideline that standardizes how post-approval drug safety data are defined, managed, and rapidly reported to health authorities to ensure ongoing monitoring of medicinal product safety.
  • D. ICH S7A Safety Pharmacology Studies for Human Pharmaceuticals
    ICH S7A Safety Pharmacology Studies for Human Pharmaceuticals is an international guideline that outlines the core nonclinical safety pharmacology studies needed to evaluate the potential undesirable effects of new drugs on vital physiological functions before human use.
  • E. Safeguards Analytical Laboratory
    The Safeguards Analytical Laboratory is an International Atomic Energy Agency (IAEA) facility that performs nuclear material and environmental sample analysis to support global nuclear safeguards and non-proliferation verification.
  • F. None of above. chosen

Provenance (2 batches)

The batch behind each pipeline step, in order, with when it ran. Timestamps are batch-level — stages were processed in waves, so the object chain (NER → NED1 → NEDg → NED2) reads in order, but predicate / elicitation batches can sit in a different wave.

Step Stage Batch ID Status When
creating Elicitation batch_69e2458426188190b58b8ab4844fe420 completed April 17, 2026, 2:36 p.m.
NER Named-entity recognition batch_69f17dcffdd88190a5f9c780c71b5053 completed April 29, 2026, 3:41 a.m.
Created at: April 17, 2026, 3:33 p.m.